A Randomised Controlled Clinical Trial to evaluate the efficacy and safety of Pramehnil Tablet an Ayurvedic formulation in management of Kaphaj Prameha w.s.r.to type 2 Diabetes Mellitus

Kirti Sachdeva1 个研究点分布在 1 个国家目标入组 90 人开始时间: 2026年2月2日最近更新: 2026年1月17日

试验速览

阶段: 3 期
状态: 尚未招募
发起方
入组人数: 90
试验地点: 1

研究概览研究设计入排标准研究者研究点记录与标识符相似试验

研究概览

简要总结

It is a randomised ,prospective ,open label ,interventional controlled clinical trial.The trial consist of two groups ,one will receive trial drug Pramehnil tablet and second group will receive control drug BGR 34. Chane in the subjective and objective parameters of kaphaj prameha or type 2 DM will be the end point of study

研究设计

研究类型: Interventional
分配方式: Randomized
盲法: None

入排标准

年龄范围: 30.00 Year(s) 至 70.00 Year(s)（—）
性别: All

入选标准

•Patient freshly diagnosed or already diagnosed between the age of 30 years to 70 years with HbA1c range between 6.5 to 9 also having symptoms pf type 2 DM or kaphaj prameha and willing to give consent for participation.

排除标准

•Patient not willing to give consent below the age of 30 and above the age of 70 with high HbA1c more than 9 also having complication of type 2 DM like neuropathy retinopathy nephrophathy also patient of type 1 DM Pancreatitis any other serious medical condition like malignancy pregnent and lactating mothers also excluded.

研究者

发起方

Kirti Sachdeva

申办方类型

Other [self]

责任方

Principal Investigator

主要研究者

Dr.Kirti Sachdeva

M.S.Regional Ayurveda Research Institute

研究点 (1)

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